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Epithelial basement membrane dystrophy ( EBMD) is a disorder of the eye that can cause pain and dryness. It is sometimes included in the group of corneal dystrophies. [ 1] It diverges from the formal definition of corneal dystrophy since it is non-familial in most cases. It also has a fluctuating course, while for a typical corneal dystrophy ...
Rheumatology. Cogan syndrome (also Cogan's syndrome) is a rare disorder characterized by recurrent inflammation of the front of the eye (the cornea) and often fever, fatigue, and weight loss, episodes of vertigo (dizziness), tinnitus (ringing in the ears) and hearing loss. It can lead to deafness or blindness if untreated.
Oculopharyngeal muscular dystrophy ( OPMD) is a rare form of muscular dystrophy with symptoms generally starting when an individual is 40 to 50 years old. It can be autosomal dominant neuromuscular disease or autosomal recessive. The most common inheritance of OPMD is autosomal dominant, which means only one copy of the mutated gene needs to be ...
Complex regional pain syndrome ( CRPS Type 1 and Type 2) is a severe form of chronic pain, in which pain from a physical trauma outlasts the expected recovery time. The symptoms of types 1 and 2 are the same except type 2 is associated with nerve injury. Usually starting in a limb, CRPS manifests as pain, swelling, limited range of motion, and ...
Polymyalgia rheumatica ( PMR) is a syndrome experienced as pain or stiffness, usually in the neck, shoulders, upper arms, and hips, but which may occur all over the body. The pain can be sudden or can occur gradually over a period. Most people with PMR wake up in the morning with pain in their muscles; however, cases have occurred in which the ...
An occurrence of central serous retinopathy of the fovea centralis imaged using optical coherence tomography. Specialty. Ophthalmology. Central serous chorioretinopathy ( CSC or CSCR ), also known as central serous retinopathy ( CSR ), is an eye disease that causes visual impairment, often temporary, usually in one eye. [ 1][ 2] When the ...
Spinal and bulbar muscular atrophy ( SBMA ), popularly known as Kennedy's disease, is a rare, adult-onset, X-linked recessive lower motor neuron disease caused by trinucleotide CAG repeat expansions in exon 1 of the androgen receptor (AR) gene, which results in both loss of AR function and toxic gain of function. [ 2][ 3] In men, the disease ...
August 9, 2024 at 10:38 AM. By Sriparna Roy and Christy Santhosh. (Reuters) -The U.S. Food and Drug Administration has approved ARS Pharmaceuticals' nasal spray as the first needle-free emergency ...
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